Packaging Process Development: Including the design and manufacture of tooling used to create blisters and sealed packages.
Sterilization Processes: ETO sterilization or gamma radiation.
Sterilization Process Validation: Each product package family has its own documented sterilization program that includes initial and ongoing validation of sterilization effectiveness.
Auditing: Our device manufacturing and sterilized barrier packaging operations are subject to audits by current and new customers, ISO, JPAL, and certified auditors on our own staff (we have six). As a result we are in a continual state of readiness for information requests and our assembly and packaging, validation, and traceability processes are continually upgraded based on audit recommendations.
Industry Failure Report Analysis: Our team continuously monitors industry mandated failure reports and evaluates how problems experienced by others can be avoided in our own device manufacturing and sterilized barrier packaging operations.
International Standards Compliance: Medical device products manufactured and packaged at Paragon Medical facilities are distributed for domestic and international customers, and we make sure our customers’ packaging meets all of regulatory standards applicable to those locations.